-
1
-
-
85043954628
-
-
For reviews of natural products containing butenolides, see
-
For reviews of natural products containing butenolides, see:
-
-
-
-
3
-
-
17844386379
-
-
A. Bermejo, B. Figadère, M.-C. Zafra-Polo, I. Barrachina, E. Estornell, D. Cortes, Nat. Prod. Rep. 2005, 22, 269;
-
(2005)
Nat. Prod. Rep.
, vol.22
, pp. 269
-
-
Bermejo, A.1
Figadère, B.2
Zafra-Polo, M.-C.3
Barrachina, I.4
Estornell, E.5
Cortes, D.6
-
7
-
-
51649086878
-
-
T. Montagnon, M. Tofi, G. Vassilikogiannakis, Acc. Chem. Res. 2008, 41, 1001;
-
(2008)
Acc. Chem. Res.
, vol.41
, pp. 1001
-
-
Montagnon, T.1
Tofi, M.2
Vassilikogiannakis, G.3
-
8
-
-
67649452262
-
-
G. Casiraghi, F. Zanardi, L. Battistini, G. Rassu, Synlett 2009, 1525;
-
(2009)
Synlett
, pp. 1525
-
-
Casiraghi, G.1
Zanardi, F.2
Battistini, L.3
Rassu, G.4
-
9
-
-
79955923795
-
-
G. Casiraghi, L. Battistini, C. Curti, G. Rassu, F. Zanardi, Chem. Rev. 2011, 111, 3076;
-
(2011)
Chem. Rev.
, vol.111
, pp. 3076
-
-
Casiraghi, G.1
Battistini, L.2
Curti, C.3
Rassu, G.4
Zanardi, F.5
-
10
-
-
84888097067
-
-
Q. Zhang, X. Liu, X. Feng, Curr. Org. Synth. 2013, 10, 764.
-
(2013)
Curr. Org. Synth.
, vol.10
, pp. 764
-
-
Zhang, Q.1
Liu, X.2
Feng, X.3
-
11
-
-
76849100414
-
-
H.-L. Cui, J.-R. Huang, J. Lei, Z.-F. Wang, S. Chen, L. Wu, Y.-C. Chen, Org. Lett. 2010, 12, 720;
-
(2010)
Org. Lett.
, vol.12
, pp. 720
-
-
Cui, H.-L.1
Huang, J.-R.2
Lei, J.3
Wang, Z.-F.4
Chen, S.5
Wu, L.6
Chen, Y.-C.7
-
12
-
-
84863115406
-
-
X. Huang, J. Peng, L. Dong, Y.-C. Chen, Chem. Commun. 2012, 48, 2439.
-
(2012)
Chem. Commun.
, vol.48
, pp. 2439
-
-
Huang, X.1
Peng, J.2
Dong, L.3
Chen, Y.-C.4
-
13
-
-
79958831670
-
-
L. Zhou, L. Lin, J. Ji, M. Xie, X. Liu, X. Feng, Org. Lett. 2011, 13, 3056.
-
(2011)
Org. Lett.
, vol.13
, pp. 3056
-
-
Zhou, L.1
Lin, L.2
Ji, J.3
Xie, M.4
Liu, X.5
Feng, X.6
-
14
-
-
85043953871
-
-
For selected examples, see
-
For selected examples, see:
-
-
-
-
15
-
-
79952594736
-
-
A. Quintard, A. Lefranc, A. Alexakis, Org. Lett. 2011, 13, 1540;
-
(2011)
Org. Lett.
, vol.13
, pp. 1540
-
-
Quintard, A.1
Lefranc, A.2
Alexakis, A.3
-
16
-
-
84860379068
-
-
M. S. Manna, V. Kumar, S. Mukherjee, Chem. Commun. 2012, 48, 5193;
-
(2012)
Chem. Commun.
, vol.48
, pp. 5193
-
-
Manna, M.S.1
Kumar, V.2
Mukherjee, S.3
-
17
-
-
84867022718
-
-
W. Zhang, D. Tan, R. Lee, G. Tong, W. Chen, B. Qi, K.-W. Huang, C.-H. Tan, Z. Jiang, Angew. Chem. Int. Ed. 2012, 51, 10069;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 10069
-
-
Zhang, W.1
Tan, D.2
Lee, R.3
Tong, G.4
Chen, W.5
Qi, B.6
Huang, K.-W.7
Tan, C.-H.8
Jiang, Z.9
-
18
-
-
84875832794
-
-
Angew. Chem. 2012, 124, 10216;
-
(2012)
Angew. Chem.
, vol.124
, pp. 10216
-
-
-
20
-
-
84895172220
-
-
J. Ji, L. Lin, L. Zhou, Y. Zhang, Y. Liu, X. Liu, X. Feng, Adv. Synth. Catal. 2013, 355, 2764;
-
(2013)
Adv. Synth. Catal.
, vol.355
, pp. 2764
-
-
Ji, J.1
Lin, L.2
Zhou, L.3
Zhang, Y.4
Liu, Y.5
Liu, X.6
Feng, X.7
-
21
-
-
84875820871
-
-
D. Yang, L. Wang, D. Zhao, F. Han, B. Zhang, R. Wang, Chem. Eur. J. 2013, 19, 4691;
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 4691
-
-
Yang, D.1
Wang, L.2
Zhao, D.3
Han, F.4
Zhang, B.5
Wang, R.6
-
22
-
-
84900837773
-
-
L. Yin, H. Takada, S. Lin, N. Kumagai, M. Shibasaki, Angew. Chem. Int. Ed. 2014, 53, 5327;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 5327
-
-
Yin, L.1
Takada, H.2
Lin, S.3
Kumagai, N.4
Shibasaki, M.5
-
23
-
-
84990246160
-
-
Angew. Chem. 2014, 126, 5431;
-
(2014)
Angew. Chem.
, vol.126
, pp. 5431
-
-
-
24
-
-
84905001758
-
-
X. Li, M. Lu, Y. Dong, W. Wu, Q. Qian, J. Ye, D. J. Dixon, Nat. Commun. 2014, 5, 4479;
-
(2014)
Nat. Commun.
, vol.5
, pp. 4479
-
-
Li, X.1
Lu, M.2
Dong, Y.3
Wu, W.4
Qian, Q.5
Ye, J.6
Dixon, D.J.7
-
26
-
-
84959017460
-
-
T. Sekikawa, T. Kitaguchi, H. Kitaura, T. Minami, Y. Hatanaka, Org. Lett. 2016, 18, 646.
-
(2016)
Org. Lett.
, vol.18
, pp. 646
-
-
Sekikawa, T.1
Kitaguchi, T.2
Kitaura, H.3
Minami, T.4
Hatanaka, Y.5
-
27
-
-
85043943695
-
-
For non-asymmetric α-addition of deconjugated butenolides, see
-
For non-asymmetric α-addition of deconjugated butenolides, see:
-
-
-
-
29
-
-
0042761806
-
-
for the Lewis acid catalyzed enantioselective α-addition of similar silyloxyfurans, see
-
A. Y. Egorova, Z. Y. Timofeeva, Russ. J. Gen. Chem. 2003, 73, 655; for the Lewis acid catalyzed enantioselective α-addition of similar silyloxyfurans, see:
-
(2003)
Russ. J. Gen. Chem.
, vol.73
, pp. 655
-
-
Egorova, A.Y.1
Timofeeva, Z.Y.2
-
30
-
-
84867531252
-
-
M. Woyciechowska, G. Forcher, S. Buda, J. Mlynarski, Chem. Commun. 2012, 48, 11029;
-
(2012)
Chem. Commun.
, vol.48
, pp. 11029
-
-
Woyciechowska, M.1
Forcher, G.2
Buda, S.3
Mlynarski, J.4
-
31
-
-
84858780363
-
-
B. Mao, Y. Ji, M. Fañanás-Mastral, G. Caroli, A. Meetsma, B. L. Feringa, Angew. Chem. Int. Ed. 2012, 51, 3168;
-
(2012)
Angew. Chem. Int. Ed.
, vol.51
, pp. 3168
-
-
Mao, B.1
Ji, Y.2
Fañanás-Mastral, M.3
Caroli, G.4
Meetsma, A.5
Feringa, B.L.6
-
32
-
-
84872417572
-
-
Angew. Chem. 2012, 124, 3222;
-
(2012)
Angew. Chem.
, vol.124
, pp. 3222
-
-
-
36
-
-
85015636155
-
-
Angew. Chem. 2010, 122, 6093;
-
(2010)
Angew. Chem.
, vol.122
, pp. 6093
-
-
-
37
-
-
79960696769
-
-
M. Nadai, F. Doria, M. Di Antonio, G. Sattin, L. Germani, C. Percivalle, M. Palumbo, S. N. Richter, M. Freccero, Biochimie 2011, 93, 1328;
-
(2011)
Biochimie
, vol.93
, pp. 1328
-
-
Nadai, M.1
Doria, F.2
Di Antonio, M.3
Sattin, G.4
Germani, L.5
Percivalle, C.6
Palumbo, M.7
Richter, S.N.8
Freccero, M.9
-
38
-
-
84860374939
-
-
F. Doria, M. Nadai, M. Folini, M. Di Antonio, L. Germani, C. Percivalle, C. Sissi, N. Zaffaroni, S. Alcaro, A. Artese, S. N. Richter, M. Freccero, Org. Biomol. Chem. 2012, 10, 2798;
-
(2012)
Org. Biomol. Chem.
, vol.10
, pp. 2798
-
-
Doria, F.1
Nadai, M.2
Folini, M.3
Di Antonio, M.4
Germani, L.5
Percivalle, C.6
Sissi, C.7
Zaffaroni, N.8
Alcaro, S.9
Artese, A.10
Richter, S.N.11
Freccero, M.12
-
39
-
-
84871533376
-
-
F. Doria, M. Nadai, M. Folini, M. Scalabrin, L. Germani, G. Sattin, M. Mella, M. Palumbo, N. Zaffaroni, D. Fabris, M. Freccero, S. N. Richter, Chem. Eur. J. 2013, 19, 78;
-
(2013)
Chem. Eur. J.
, vol.19
, pp. 78
-
-
Doria, F.1
Nadai, M.2
Folini, M.3
Scalabrin, M.4
Germani, L.5
Sattin, G.6
Mella, M.7
Palumbo, M.8
Zaffaroni, N.9
Fabris, D.10
Freccero, M.11
Richter, S.N.12
-
40
-
-
84892970081
-
-
C. Percivalle, F. Doria, M. Freccero, Curr. Org. Chem. 2014, 18, 19.
-
(2014)
Curr. Org. Chem.
, vol.18
, pp. 19
-
-
Percivalle, C.1
Doria, F.2
Freccero, M.3
-
43
-
-
72249092522
-
-
S. B. Ferreira, F. de C. da Silva, A. C. Pinto, D. T. G. Gonzaga, V. F. Ferreira, J. Heterocycl. Chem. 2009, 46, 1080;
-
(2009)
J. Heterocycl. Chem.
, vol.46
, pp. 1080
-
-
Ferreira, S.B.1
da Silva, F.C.2
Pinto, A.C.3
Gonzaga, D.T.G.4
Ferreira, V.F.5
-
45
-
-
84918518265
-
-
W.-J. Bai, J. G. David, Z.-G. Feng, M. G. Weaver, K.-L. Wu, T. R. R. Pettus, Acc. Chem. Res. 2014, 47, 3655;
-
(2014)
Acc. Chem. Res.
, vol.47
, pp. 3655
-
-
Bai, W.-J.1
David, J.G.2
Feng, Z.-G.3
Weaver, M.G.4
Wu, K.-L.5
Pettus, T.R.R.6
-
46
-
-
84908611385
-
-
M. S. Singh, A. Nagaraju, N. Anand, S. Chowdhury, RSC Adv. 2014, 4, 55924;
-
(2014)
RSC Adv.
, vol.4
, pp. 55924
-
-
Singh, M.S.1
Nagaraju, A.2
Anand, N.3
Chowdhury, S.4
-
47
-
-
84942323219
-
-
W. Ai, D. Liao, X. Lei, Chin. J. Org. Chem. 2015, 35, 1615.
-
(2015)
Chin. J. Org. Chem.
, vol.35
, pp. 1615
-
-
Ai, W.1
Liao, D.2
Lei, X.3
-
48
-
-
85043870542
-
-
For recent reviews, see
-
For recent reviews, see:
-
-
-
-
50
-
-
84938635862
-
-
L. Caruana, M. Fochi, L. Bernardi, Molecules 2015, 20, 11733;
-
(2015)
Molecules
, vol.20
, pp. 11733
-
-
Caruana, L.1
Fochi, M.2
Bernardi, L.3
-
52
-
-
85043899527
-
-
For transition-metal catalysis involving o-QMs, see
-
For transition-metal catalysis involving o-QMs, see:
-
-
-
-
54
-
-
72249086147
-
-
K. H. Jensen, T. P. Pathak, Y. Zhang, M. S. Sigman, J. Am. Chem. Soc. 2009, 131, 17074;
-
(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 17074
-
-
Jensen, K.H.1
Pathak, T.P.2
Zhang, Y.3
Sigman, M.S.4
-
55
-
-
77953298188
-
-
T. P. Pathak, K. M. Gligorich, B. E. Welm, M. S. Sigman, J. Am. Chem. Soc. 2010, 132, 7870;
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 7870
-
-
Pathak, T.P.1
Gligorich, K.M.2
Welm, B.E.3
Sigman, M.S.4
-
56
-
-
78650113123
-
-
K. H. Jensen, J. D. Webb, M. S. Sigman, J. Am. Chem. Soc. 2010, 132, 17471;
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 17471
-
-
Jensen, K.H.1
Webb, J.D.2
Sigman, M.S.3
-
57
-
-
84865273140
-
-
R. Jana, T. P. Pathak, K. H. Jensen, M. S. Sigman, Org. Lett. 2012, 14, 4074;
-
(2012)
Org. Lett.
, vol.14
, pp. 4074
-
-
Jana, R.1
Pathak, T.P.2
Jensen, K.H.3
Sigman, M.S.4
-
59
-
-
84923212034
-
-
H. Hu, Y. Liu, J. Guo, L. Lin, Y. Xu, X. Liu, X. Feng, Chem. Commun. 2015, 51, 3835.
-
(2015)
Chem. Commun.
, vol.51
, pp. 3835
-
-
Hu, H.1
Liu, Y.2
Guo, J.3
Lin, L.4
Xu, Y.5
Liu, X.6
Feng, X.7
-
60
-
-
85043922504
-
-
For selected examples of organocatalysis involving o-QMs, see
-
For selected examples of organocatalysis involving o-QMs, see:
-
-
-
-
61
-
-
58149175558
-
-
E. Alden-Danforth, M. T. Scerba, T. Lectka, Org. Lett. 2008, 10, 4951;
-
(2008)
Org. Lett.
, vol.10
, pp. 4951
-
-
Alden-Danforth, E.1
Scerba, M.T.2
Lectka, T.3
-
63
-
-
84880835415
-
-
H. Lv, W.-Q. Jia, L.-H. Sun, S. Ye, Angew. Chem. Int. Ed. 2013, 52, 8607;
-
(2013)
Angew. Chem. Int. Ed.
, vol.52
, pp. 8607
-
-
Lv, H.1
Jia, W.-Q.2
Sun, L.-H.3
Ye, S.4
-
64
-
-
84925148269
-
-
Angew. Chem. 2013, 125, 8769;
-
(2013)
Angew. Chem.
, vol.125
, pp. 8769
-
-
-
65
-
-
84880764620
-
-
J. Izquierdo, A. Orue, K. A. Scheidt, J. Am. Chem. Soc. 2013, 135, 10634;
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 10634
-
-
Izquierdo, J.1
Orue, A.2
Scheidt, K.A.3
-
66
-
-
84904704883
-
-
O. El-Sepelgy, S. Haseloff, S. K. Alamsetti, C. Schneider, Angew. Chem. Int. Ed. 2014, 53, 7923;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 7923
-
-
El-Sepelgy, O.1
Haseloff, S.2
Alamsetti, S.K.3
Schneider, C.4
-
67
-
-
84969370601
-
-
Angew. Chem. 2014, 126, 8057;
-
(2014)
Angew. Chem.
, vol.126
, pp. 8057
-
-
-
68
-
-
84915749984
-
-
C.-C. Hsiao, H.-H. Liao, M. Rueping, Angew. Chem. Int. Ed. 2014, 53, 13258;
-
(2014)
Angew. Chem. Int. Ed.
, vol.53
, pp. 13258
-
-
Hsiao, C.-C.1
Liao, H.-H.2
Rueping, M.3
-
69
-
-
84969375432
-
-
Angew. Chem. 2014, 126, 13474;
-
(2014)
Angew. Chem.
, vol.126
, pp. 13474
-
-
-
70
-
-
84921022287
-
-
Z. Wang, F. Ai, Z. Wang, W. Zhao, G. Zhu, Z. Lin, J. Sun, J. Am. Chem. Soc. 2015, 137, 383;
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 383
-
-
Wang, Z.1
Ai, F.2
Wang, Z.3
Zhao, W.4
Zhu, G.5
Lin, Z.6
Sun, J.7
-
71
-
-
85027918784
-
-
W. Zhao, Z. Wang, B. Chu, J. Sun, Angew. Chem. Int. Ed. 2015, 54, 1910;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 1910
-
-
Zhao, W.1
Wang, Z.2
Chu, B.3
Sun, J.4
-
72
-
-
84969386046
-
-
Angew. Chem. 2015, 127, 1930;
-
(2015)
Angew. Chem.
, vol.127
, pp. 1930
-
-
-
73
-
-
85027932744
-
-
J.-J. Zhao, S.-B. Sun, S.-H. He, Q. Wu, F. Shi, Angew. Chem. Int. Ed. 2015, 54, 5460;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 5460
-
-
Zhao, J.-J.1
Sun, S.-B.2
He, S.-H.3
Wu, Q.4
Shi, F.5
-
74
-
-
84969375422
-
-
Angew. Chem. 2015, 127, 5550;
-
(2015)
Angew. Chem.
, vol.127
, pp. 5550
-
-
-
75
-
-
84929501074
-
-
C.-C. Hsiao, S. Raja, H.-H. Liao, I. Atodiresei, M. Rueping, Angew. Chem. Int. Ed. 2015, 54, 5762;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 5762
-
-
Hsiao, C.-C.1
Raja, S.2
Liao, H.-H.3
Atodiresei, I.4
Rueping, M.5
-
76
-
-
84969385712
-
-
Angew. Chem. 2015, 127, 5854;
-
(2015)
Angew. Chem.
, vol.127
, pp. 5854
-
-
-
77
-
-
84926322836
-
-
W. Guo, B. Wu, X. Zhou, P. Chen, X. Wang, Y.-G. Zhou, Y. Liu, C. Li, Angew. Chem. Int. Ed. 2015, 54, 4522;
-
(2015)
Angew. Chem. Int. Ed.
, vol.54
, pp. 4522
-
-
Guo, W.1
Wu, B.2
Zhou, X.3
Chen, P.4
Wang, X.5
Zhou, Y.-G.6
Liu, Y.7
Li, C.8
-
78
-
-
84969385723
-
-
Angew. Chem. 2015, 127, 4605.
-
(2015)
Angew. Chem.
, vol.127
, pp. 4605
-
-
-
79
-
-
84873280354
-
-
M.-W. Chen, L.-L. Cao, Z.-S. Ye, G.-F. Jiang, Y.-G. Zhou, Chem. Commun. 2013, 49, 1660;
-
(2013)
Chem. Commun.
, vol.49
, pp. 1660
-
-
Chen, M.-W.1
Cao, L.-L.2
Ye, Z.-S.3
Jiang, G.-F.4
Zhou, Y.-G.5
-
80
-
-
84899926526
-
-
B. Wu, M.-W. Chen, Z.-S. Ye, C.-B. Yu, Y.-G. Zhou, Adv. Synth. Catal. 2014, 356, 383;
-
(2014)
Adv. Synth. Catal.
, vol.356
, pp. 383
-
-
Wu, B.1
Chen, M.-W.2
Ye, Z.-S.3
Yu, C.-B.4
Zhou, Y.-G.5
-
81
-
-
84941078238
-
-
B. Wu, X. Gao, M.-W. Chen, Y.-G. Zhou, Chin. J. Chem. 2014, 32, 981;
-
(2014)
Chin. J. Chem.
, vol.32
, pp. 981
-
-
Wu, B.1
Gao, X.2
Chen, M.-W.3
Zhou, Y.-G.4
-
82
-
-
84922551109
-
-
B. Wu, X. Gao, M.-W. Chen, Y.-G. Zhou, Tetrahedron Lett. 2015, 56, 1135;
-
(2015)
Tetrahedron Lett.
, vol.56
, pp. 1135
-
-
Wu, B.1
Gao, X.2
Chen, M.-W.3
Zhou, Y.-G.4
-
83
-
-
84930925764
-
-
B. Wu, X. Gao, Z. Yan, W.-X. Huang, Y.-G. Zhou, Tetrahedron Lett. 2015, 56, 4334;
-
(2015)
Tetrahedron Lett.
, vol.56
, pp. 4334
-
-
Wu, B.1
Gao, X.2
Yan, Z.3
Huang, W.-X.4
Zhou, Y.-G.5
-
84
-
-
84952690837
-
-
B. Wu, X. Gao, Z. Yan, M.-W. Chen, Y.-G. Zhou, Org. Lett. 2015, 17, 6134.
-
(2015)
Org. Lett.
, vol.17
, pp. 6134
-
-
Wu, B.1
Gao, X.2
Yan, Z.3
Chen, M.-W.4
Zhou, Y.-G.5
-
85
-
-
0004102743
-
-
Wiley, New York
-
R. D. H. Murray, J. Mendez, S. A. Brown, The Natural Coumarin: Occurrence, Chemistry, and Biochemistry, Wiley, New York, 1982;
-
(1982)
The Natural Coumarin: Occurrence, Chemistry, and Biochemistry
-
-
Murray, R.D.H.1
Mendez, J.2
Brown, S.A.3
-
86
-
-
0003765137
-
-
1, st ed.,, Wiley, Chichester
-
R. O'Kennedy, R. D. Thornes, Coumarins: Biology, Applications, and Mode of Action, 1st ed., Wiley, Chichester, 1997;
-
(1997)
Coumarins: Biology, Applications, and Mode of Action
-
-
O'Kennedy, R.1
Thornes, R.D.2
-
88
-
-
85043967651
-
-
See the Supporting Information for details. When sodium carbonate was used as the base, the reaction did not occur. With potassium carbonate as the base, only a side product was obtained
-
See the Supporting Information for details. When sodium carbonate was used as the base, the reaction did not occur. With potassium carbonate as the base, only a side product was obtained.
-
-
-
-
89
-
-
85043909561
-
-
CCDC 1450126 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre
-
CCDC 1450126 contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre.
-
-
-
-
90
-
-
85043967335
-
-
See Figure S1 in the Supporting Information for the full Gibbs free energy profiles of the reaction
-
See Figure S1 in the Supporting Information for the full Gibbs free energy profiles of the reaction.
-
-
-
-
94
-
-
84897055356
-
-
A. G. Green, P. Liu, C. A. Merlic, K. N. Houk, J. Am. Chem. Soc. 2014, 136, 4575;
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 4575
-
-
Green, A.G.1
Liu, P.2
Merlic, C.A.3
Houk, K.N.4
-
95
-
-
84954445605
-
-
T. Wang, Z. Yu, D. L. Hoon, C. Y. Phee, Y. Lan, Y. Lu, J. Am. Chem. Soc. 2016, 138, 265.
-
(2016)
J. Am. Chem. Soc.
, vol.138
, pp. 265
-
-
Wang, T.1
Yu, Z.2
Hoon, D.L.3
Phee, C.Y.4
Lan, Y.5
Lu, Y.6
|